Visitor Monitoring Drug History: HEPARIN LOCK FLUSH
 
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Label and Approval History

Drug Name: HEPARIN LOCK FLUSH
FDA Application No: (NDA) 017029
Active Ingredient(s): HEPARIN SODIUM
Company: ABRAXIS PHARM
 
Label History
 
Labels are not available on this site for HEPARIN LOCK FLUSH, (NDA) 017029
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/22/2002 099Labeling Revision Letter 
12/13/1999 098Manufacturing Change or Addition  
3/8/2000 097Package Change  
11/4/1997 096Control Supplement  
6/24/1997 095Control Supplement  
8/6/1998 094Manufacturing Change or Addition  
5/17/1995 084Manufacturing Change or Addition  
10/27/1994 078Manufacturing Change or Addition  
7/26/1996 073Control Supplement  
8/25/1993 069Labeling Revision  
8/6/1998 063Manufacturing Change or Addition  
8/6/1998 062Manufacturing Change or Addition  
6/8/1989 061Package Change  
9/22/1988 060Labeling Revision  
2/16/1988 058Control Supplement  
12/1/1989 057Package Change  
6/26/1992 056Labeling Revision  
4/28/1986 054Control Supplement  
4/7/1986 053Labeling Revision  
9/22/1987 051Package Change  
9/22/1987 050Package Change  
7/29/1985 049General Efficacy (MarkIV)  
11/6/1984 048Package Change  
12/5/1985 047Package Change  
12/5/1985 046Package Change  
12/5/1985 045Package Change  
12/5/1985 044Package Change  
12/5/1985 043Package Change  
12/5/1985 042Package Change  
11/2/1983 041Formulation Revision  
11/2/1983 040Formulation Revision  
11/2/1983 039Formulation Revision  
11/2/1983 038Formulation Revision  
5/16/1985 037Formulation Revision  
11/2/1983 036Formulation Revision  
11/2/1983 034Expiration Date Change  
1/4/1983 033Expiration Date Change  
9/21/1982 032Manufacturing Change or Addition  
9/21/1982 031Manufacturing Change or Addition  
5/6/1982 030Labeling Revision  
9/17/1982 029Control Supplement  
2/24/1981 027Labeling Revision  
3/24/1981 026Manufacturing Change or Addition  
10/31/1979 025Control Supplement  
10/31/1979 024Manufacturing Change or Addition  
11/21/1978 023Control Supplement  
11/21/1978 022Control Supplement  
5/23/1978 021Labeling Revision  
12/14/1977 020Control Supplement  
12/3/1976 019Control Supplement  
12/3/1976 017Formulation Revision  
1/26/1977 016Formulation Revision  
12/4/1977 015Labeling Revision  
6/16/1976 014Manufacturing Change or Addition  
2/9/1976 012Labeling Revision  
1/9/1976 011Control Supplement  
1/9/1976 010Formulation Revision  
3/17/1976 009Control Supplement  
2/9/1976 008Control Supplement  
8/29/1975 007Control Supplement  
2/22/1972 000Approval  
 
Therapeutic Equivalents
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